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10-Hydroxycamptothecin

10-Hydroxycamptothecin Structure
CAS No.
19685-09-7
Chemical Name:
10-Hydroxycamptothecin
Synonyms
SN38;HCPT;HYDROXYCAMPTOTHECIN;10-HCPT;(S)-10-HYDROXYCAMPTOTHECIN;Ampule;NSC 107124;HYDROCAMPTOTHECINE;hydroxy-camptotheci;Irinotecan USP RC A
CBNumber:
CB4445430
Molecular Formula:
C20H16N2O5
Molecular Weight:
364.35
MOL File:
19685-09-7.mol
MSDS File:
SDS
Modify Date:
2023/6/8 9:02:14

10-Hydroxycamptothecin Properties

Melting point 265-270°C
Boiling point 820.7±65.0 °C(Predicted)
Density 1.60
storage temp. Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
solubility ≥23.8 mg/mL in DMSO with gentle warming; insoluble in EtOH; insoluble in H2O
form powder to crystal
pka 8.93±0.40(Predicted)
color White to Yellow to Orange
InChIKey HAWSQZCWOQZXHI-FQEVSTJZSA-N
CAS DataBase Reference 19685-09-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS08
Signal word  Danger
Hazard statements  H301-H340
Precautionary statements  P202-P264-P270-P280-P301+P310-P405
Safety Statements  24/25
HS Code  29349990
NFPA 704
0
2 0

10-Hydroxycamptothecin price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) PHR2491 Irinotecan Related Compound A certified reference material, pharmaceutical secondary standard 19685-09-7 25MG ₹44804.68 2022-06-14 Buy
TCI Chemicals (India) H1463 10-Hydroxycamptothecin 19685-09-7 1G ₹14200 2022-05-26 Buy
Product number Packaging Price Buy
PHR2491 25MG ₹44804.68 Buy
H1463 1G ₹14200 Buy

10-Hydroxycamptothecin Chemical Properties,Uses,Production

Description

DNA topoisomerases relax supercoiled DNA during replication, transcription, recombination, repair, and chromosome condensation. The relaxation of DNA supercoiling by topoisomerase I at single-strand breaks represents a target for anticancer agents to intercalate between DNA base pairs, leading to the activation of apoptotic and cell cycle arrest pathways. (S)-10-hydroxy-Camptothecin is an inhibitor of topoisomerase I originally isolated from the Chinese tree C. acuminata. It is a member of the camptothecin family that demonstrates less toxicity than its parent compound. (S)-10-hydroxy-Camptothecin has strong anti-tumor activity against a wide range of experimental tumors including L1210 leukemia cells (IC50 = 1.15 μM). In vitro treatment of human HepG2 cells with 5-20 μM (S)-10-hydroxy-camptothecin results in cell cycle arrest at the G2/M phase.

Chemical Properties

Yellow Solid

Uses

A Camptothecin derivative; a topoisomerase inhibitor for cancer therapy

10-Hydroxycamptothecin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 468)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
JSK Chemicals +919879767970 Gujarat, India 3756 58 Inquiry
Rivashaa Agrotech Biopharma Pvt. Ltd. +91-26463395 +91-7926462688 Gujarat, India 1615 58 Inquiry
Avra Laboratories Pvt Ltd +91-8008572391 +91-8008572391 Hyderabad, India 43 58 Inquiry
SynZeal Research Pvt Ltd +1 226-802-2078 Gujarat, India 6522 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
AVRA LABORATORIES PRIVATE LTD +91-040- 27178571 New Delhi, India 3 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Manus Aktteva +91 (79) 6512-3395 New Delhi, India 581 34 Inquiry
VIVAN Life Sciences Pvt. Limited. +91(22) 2544 4584 / 2544 4585 New Delhi, India 138 50 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry

10-Hydroxycamptothecin Spectrum

Camptothecae Acuminatae extract hydrate,(s)-dihydroxy hydroxy-camptotheci Hydroxycamptothencine (20S)-10-HYDROXYCAMPTOTHECIN 98% (20S)-10-Hydroxycamptothecin HYDROCAMPTOTHECINE CAMPTOTHECIN, 10-HYDROXY(SH) HYDROXYCAMPTOTHECIN, 10-(P) 10-hydroxycamptothecin (TECANS) 10-HYDROCAMPTOTHECIN Ampule (4S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione NSC 107124 1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione,4-ethyl-4,10-dihydroxy-, (4S)- (4S)-4,9-Dihydroxy-4-ethyl-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione 1H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione, 4-ethyl-4,9-dihydroxy-, (4S)- (S)-10-Hydroxycamptothecin (4S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione Irinotecan USP RC A CAMPTOTHECIN, 10-HYDROXY- CAMPTOTHECIN, 10-HYDROXY-, CAMPTOTHECA ACUMINATA HYDROXYCAMPTOTHECIN, 10- (20S)-10-HYDROXYCAMPTOTHECIN (20S)-7-ETHYL-10-HYDROXYCAMPTOTHECIN (S)-10-HYDROXYCAMPTOTHECIN CaMptothecin IMpurity CaMptothecin 10-Hydroxy IMpurity 10-HydroxycaMptothecin, froM Taxus chinensis (s)-10-hydroxycamptothecinhydrate 4’:6,7)indolizino(1,2-b)quinoline-3,14(4h,12h)-dione,4-ethyl-4,9-1h-pyrano(3 4’:6,7)indolizino(1,2-b)quinoline-3,14(4h,12h)-dione,4-ethyl-4,9-dihydroxy-,hydrate,(s)-1h-pyrano(3 (4S)-4α-Ethyl-4,9-dihydroxy-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14-dione (4S)-9-Hydroxy-4-hydroxy-4-ethyl-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione 10-Hydroxycamptothecin 10-Hydroxycamptothecine HYDROXYCAMPTOTHECIN, 10-(RG) 10-hydroxycamptothecin,HCPT (S)-4-Ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14-(4H,12H)-dione Irinotecan Related CoMpound A (+/-)-4-ethyl-4,9-dihydroxy-1h-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4h,12h)-dione Irinotecan Related Compound A (10 mg) ((S)-4-ethyl-4,9-dihydroxy-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione) 1H-pyrano[3',4':6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)-dione 10-HydroxycaMptothecin, HydroxycaMptothecine 10-Hydroxycamptothecin, 98%, from Taxus chinensis (Pilg.) Rehder Irinotecan Impurity 12 Irinotecan EP Impurity B 10-Hydroxycamptothecin 19685-09-7 (S)-4-ethyl-4,9-dihydroxy-1H-pyrano 10-HYDROXY CAMPTOTHECIN (IRINOTECAN EP IMPURITY B) Fructus Camptothecae Hydroxycamptothecin 80-98% (S)-10-Hydroxycamptothecin,>98% (20S)-10-Hydroxycamptothecine Camptotheca acuminata fruit extract (19S)-19-ethyl-7,19-dihydroxy-17-oxa-3,13-diazapentacyclo[11.8.0.0^{2,11}.0^{4,9}.0^{15,20}]henicosa-1(21),2,4,6,8,10,15(20)-heptaene-14,18-dione 1-Hydroxy camptothecin 10 hydroxy CamptothecinQ: What is 10 hydroxy Camptothecin Q: What is the CAS Number of 10 hydroxy Camptothecin Q: What is the storage condition of 10 hydroxy Camptothecin Irinotecan Related Compound A ((S)-4-ethyl-4,9-dihydroxy-1H-pyrano[3'',4'':6,7]indolizino[1,2-b]quino (1347610) (S)-10-HYDROXYCAMPTOTHECIN SN38